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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50866Erstellt: 24. Oktober 2026

Ethanol → 6-Hydroxy-2-(4-hydroxyphenyl)-3-(4-(2-piperidinoethoxy)-benzoyl]benzo[b]thiophene Hydrochloride 1,2-Dichloroethane

https://huagongshe.com/de/reaction/50866

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktMethanolHCID 887—
EduktBoron TrichlorideHCID 25135—
EduktRaloxifene Bismethyl Ether (hydrochloride)HCID 45260096—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt6-Hydroxy-2-(4-hydroxyphenyl)-3-(4-(2-piperidinoethoxy)-benzoyl]benzo[b]thiophene Hydrochloride 1,2-DichloroethaneHCID 9916879—

Reaktionsbedingungen

Temperatur35 °C

Reaktionsschritte

A solution of 6-methoxy -2-(4-methoxyphenyl)-3-[4-(2-piperidinylethoxy)benzoyl]benzo[b]thiophene hydrochloride (2.0 g) in 1,2-dichloroethane (20 mL) was treated with boron trichloride (2.0 mL). The resulting mixture was stirred at 35° C. for about 18 hours. A:mixture of ethanol and methanol (10 mL, 95:5, 3A) was treated with the reaction mixture from above, causing the alcoholic mixture to reflux. Upon complete addition, the resulting crystalline slurry was stirred at 25° C. After one 1 hour, the crystalline product was filtered, washed with cold ethanol (10 mL), and dried at 40° C. in vacuo to give 1.78 g of the title compound. The X-ray powder diffraction pattern is identical to that reported in Table 1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713494B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-60db984ddf1c46718e7c16f6fef6eee1
Quellennotizuspto-grants-2004_03